Analytical Science Associate & Analytical ScienceSpecialist
Onsite days role
RK26463
Contract 11 months initially
Carlow



We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


Theseroles are responsible for supporting Analytical Procedure Life Cycle through end-to-end method lifecycle management including introduction of new analytical methods, analytical transfers, SME assessment for all analytical method & equipment performance qualification, investigations, product testing and technical rationale.


Key Responsibilities:

• Support/Lead analytical method transfers, validations, and compendial method verifications.
• Perform laboratory-based analytical testing and technical studies using a variety of analytical techniques and instrumentation.
• Generate, review, interpret, and verify analytical data and technical documentation.
• Support lifecycle management and continuous improvement of analytical methods.
• Assist with troubleshooting of analytical methods and laboratory equipment.
• Support equipment performance qualification activities (PQ).
• Participate in laboratory investigations, deviations, CAPAs, and change controls.
• Collaborate with Quality Control, Manufacturing, Validation, Technical Operations, and Global Analytical teams.
• Ensure compliance with cGMP, data integrity, safety, and regulatory requirements.
• Supporting digital method development.

• Bachelor's Degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum 2-3 years' experiencefor Associate level and 3-5 years' experiencefor Specialist level within the pharmaceutical, biotechnology, or vaccine industry.
• Experience working in a GMP-regulated laboratory environment.
• Experience with analytical testing, data review, and technical documentation.
• Experience with method validation, method transfer, compendial testing, chromatography, electrophoresis, ELISA or analytical troubleshooting is advantageous.